Skip directly to search
Skip directly to A to Z list
Skip directly to navigation
Skip directly to page options
Skip directly to site content
Start of Search Controls
Search Form Controls
Search The CDC
submit
CDC A-Z Index
MENU
CDC A-Z
SEARCH
A
B
C
D
E
F
G
H
I
J
K
L
M
N
O
P
Q
R
S
T
U
V
W
X
Y
Z
#
Search Form Controls
Search The CDC
submit
CDC A-Z Index
Public Health Genomics and Precision Health Knowledge Base (v8.7)
PHGKB
About
Office of Genomics and Precision Public Health
Genomics (A-Z)
Specialized PHGKB
Cancer PHGKB
Diabetes PHGKB
Economic Evaluation PHGKB
Environmental Health PHGKB
Family Health History PHGKB
Health Equity PHGKB
HLBS-PopOmics
Infectious Diseases PHGKB
Implementation Science PHGKB
Neurological Disorders PHGKB
Pharmacogenomics PHGKB
Primary Immune Deficiency Diseases PHGKB
Rare Diseases PHGKB
Reproductive and Child Health PHGKB
Genomics Precision Health Scan
(Current Edition)
Advanced Molecular Detection Clips
(Current Edition)
Non-Genomics Precision Health Scan
(Current Edition)
CDC-Authored Precision Health Publications Update
All Databases
COVID-19 GPH (46285)
CDC/NIH Web Information Database (31773)
CDC-Authored Genomics and Precision Health Publications Database (4409)
Precision Health Database (61629)
Tier-Classified Guidelines Database (529)
Pathogen Advanced Molecular Detection Database (25560)
All of Us Reports and Publications Database (460)
Human Genome Epidemiology
Human Genome Epidemiology Literature Finder (221382)
Epigenetic Epidemiology Publications Database (21716)
Release Note
Contact Us
Precision Health Database
Precision Health Database|Search|PHGKB
Family Health History
Last data update: Sep 22, 2023
. (Total: 61629 Documents since 2012)
All
Cancer
Diabetes
Economic
Equity
Environmental
FHH
HLBS
ID
Implementation
ND
PGx
PI
Rare
RCH
dataset
All
GPH
Non-GPH
Filtered By
:
Select to fine-tune your search
Disease
Gene
Product Type
Category
Year
Previous
Records 1 - 30 (of 583 Records)
Next
Query Trace:
all[original query]>>Reviews/Commentaries[Product Type]
Experts say Found’s story highlights the extraordinary complexity of the problem for pregnant people living with SCD – and the critical importance of receiving proper, specialized care as early as possible. This is especially true now that medical advances in care and disease-modifying therapies have helped many people living with SCD survive well through their reproductive years. For parents-to-be, that means awareness is key. Individuals with SCD are at higher risk than the general population for preeclampsia, as Found discovered; but those with preeclampsia can go on to develop a condition called eclampsia, which can lead to seizures and even coma. People with SCD are also at higher risk for sepsis and blood clots. And there are risks for the fetus, such as lower-than-normal growth in the womb, preterm delivery, and stillbirth.
K Miller, Self, September 2023
Conducting inclusive research in genetics for transgender, gender-diverse, and sex-diverse individuals: Case analyses and recommendations from a clinical genomics study.
Harris T Bland et al. J Genet Couns 2023
Similar articles in PubMed
Is Lipoprotein(a) Clinically Actionable with Today's Evidence? The Answer is Yes.
Gary S Ma et al. Curr Cardiol Rep 2023
Similar articles in PubMed
Principles of Genetic Counseling in Inherited Heart Conditions.
Susan Christian et al. Card Electrophysiol Clin 2023 15(3) 229-239
Similar articles in PubMed
Are You Up to Date on Your Preventive Care?
CDC, July 2023
Talking About Your Family History of Cancer
CDC, July 2023
Family history can help identify health risks, but many Latino people know little about theirs
L Medrano, American Heart News, June 2023
Genetic Risk Scores and Missing Heritability in Ovarian Cancer.
Yasaman Fatapour et al. Genes 2023 14(3)
Similar articles in PubMed
Are population level familial risks and germline genetics meeting each other?
Kari Hemminki et al. Hereditary cancer in clinical practice 2023 21(1) 3
Similar articles in PubMed
Expanding Family Health History to Include Family Medication History
SB Haga et al, J Per Med, Feb 2023
The Role of Genetic Testing in Patients with Heritable Thoracic Aortic Diseases.
Emanuele Monda et al. Diagnostics (Basel, Switzerland) 2023 13(4)
Similar articles in PubMed
Sudden cardiac death in the young: An update for NPs.
Julianne Doucette et al. The Nurse practitioner 2023 48(3) 21-28
Similar articles in PubMed
A Focused Clinical Review of Lynch Syndrome.
Demetra Georgiou et al. Cancer management and research 2023 1567-85
Similar articles in PubMed
Willingness to Pay for Down Syndrome Screening: A systematics Review.
Shima Nikjoo et al. Medical journal of the Islamic Republic of Iran 2023 36149
Similar articles in PubMed
Negative Molecular Diagnostics in Non-Syndromic Hearing Loss: What Next?
Clabout Thomas et al. Genes 2023 14(1)
Similar articles in PubMed
FAMILIAL PANCREATIC CANCER.
Nero Lorenzo Del et al. Clinics and research in hepatology and gastroenterology 2023 102079
Similar articles in PubMed
At What Age Should We Stop Colorectal Cancer Screening? When Is Enough, Enough?
Lieberman David et al. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2023 32(1) 6-8
Similar articles in PubMed
Genetic testing women with newly diagnosed breast cancer: What criteria are the most predictive of a positive test?
Metcalfe Kelly A et al. Cancer medicine 2022
Similar articles in PubMed
Increasing Use and Impact of Family Health History in Medically Underserved Populations: Work in Progress
G Wood et al, CDC Blog Post, December 20, 2022
Hypertrophic Cardiomyopathy (HCM) and Family Health History of Sudden Death
CDC, December 2022
Cystic Kidney Diseases That Require a Differential Diagnosis from Autosomal Dominant Polycystic Kidney Disease (ADPKD).
Sekine Akinari et al. Journal of clinical medicine 2022 11(21)
Similar articles in PubMed
Advances and Applications of Polygenic Scores for Coronary Artery Disease.
Patel Aniruddh P et al. Annual review of medicine 2022
Similar articles in PubMed
Approach Toward Germline Predisposition Syndromes in Patients with Hematologic Malignancies.
Atluri Himachandana et al. Current hematologic malignancy reports 2022
Similar articles in PubMed
When It Comes to Breast Cancer, Sometimes It’s All in the Family
G Miller, CDC Cancer, Blog, October 2022
Genetic testing for patients at risk of hereditary breast and ovarian cancer.
DeTroye Alisha et al. JAAPA : official journal of the American Academy of Physician Assistants 2022 35(10) 48-52
Similar articles in PubMed
Familial Pancreatic Cancer.
Saba Helena et al. Gastroenterology clinics of North America 2022 51(3) 561-575
Similar articles in PubMed
The Evolving Paradigm of Germline Testing in Pancreatic Ductal Adenocarcinoma and Implications for Clinical Practice.
Mohindroo Chirayu et al. Surgical pathology clinics 2022 15(3) 491-502
Similar articles in PubMed
Familial colorectal cancer.
Mangas-Sanjuan Carolina et al. Best practice & research. Clinical gastroenterology 2022 58-59101798
Similar articles in PubMed
FHH Quick App Review: How Can a Quality Review Process Assist Primary Care Providers in Choosing a Family Health History App for Patient Care?
GM Wood et al, Genes, August 2022
Genetic counseling for prion disease: Updates and best practices.
Goldman Jill S et al. Genetics in medicine : official journal of the American College of Medical Genetics 2022
Similar articles in PubMed
File Formats Help:
How do I view different file formats (PDF, DOC, PPT, MPEG) on this site?
Adobe PDF file
Microsoft PowerPoint file
Microsoft Word file
Microsoft Excel file
Audio/Video file
Apple Quicktime file
RealPlayer file
Text file
Zip Archive file
SAS file
ePub file
Page last reviewed:
Feb 1, 2023
Page last updated:
Sep 22, 2023
Content source:
Office of Genomics and Precision Public Health
,
CDC Office of Science
TOP